FDA 510(k)

On Call Pro Blood Glucose Monitoring System

N.º K: K161867 · 2016-08-05

Fecha de decisión2016-08-05

Código de productoNBW

Comité asesorCH

DecisiónSubstantially Equivalent

Resumen del dispositivo

On Call Pro Blood Glucose Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Acon Laboratories. It received FDA 510(k) clearance on 2016-08-05 under 510(k) number K161867. The device is classified under product code NBW. It was reviewed by the CH advisory panel. Product code NBW falls under the category of OB/GYN, which includes obstetric and gynecological diagnostic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the On Call Pro Blood Glucose Monitoring System?

On Call Pro Blood Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2016-08-05. The listed applicant is Acon Laboratories. The 510(k) number is K161867.

When did On Call Pro Blood Glucose Monitoring System receive FDA 510(k) clearance?

On Call Pro Blood Glucose Monitoring System received FDA 510(k) clearance on 2016-08-05, under 510(k) number K161867.

Who is the listed applicant for On Call Pro Blood Glucose Monitoring System?

The FDA 510(k) record lists Acon Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for On Call Pro Blood Glucose Monitoring System?

The FDA product code for On Call Pro Blood Glucose Monitoring System is NBW. This falls under the OB/GYN category.

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Fuente oficial

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